Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait. Shaeffer, J R, DeSimone, J, & Kleve, L J Biochem Genet, 13(11-12):783–788, 1975. Place: UNITED STATES ISBN: 0006-2928
abstract   bibtex   
The ratio of total globin alpha to beta chain synthesis was determined in reticulocytes isolated from the blood of the members of a black family, some of whom had sickle cell trait with low blood HbS concentrations (25-30%). The results support the hypothesis that sickle cell trait individuals with low HbS concentrations also carry a gene for alpha-thalassemia.
@article{shaeffer_hemoglobin_1975,
	title = {Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.},
	volume = {13},
	abstract = {The ratio of total globin alpha to beta chain synthesis was determined in reticulocytes isolated from the blood of the members of a black family, some of whom had sickle cell trait with low blood HbS concentrations (25-30\%). The results support the hypothesis that sickle cell trait individuals with low HbS concentrations also carry a gene for alpha-thalassemia.},
	language = {eng},
	number = {11-12},
	journal = {Biochem Genet},
	author = {Shaeffer, J R and DeSimone, J and Kleve, L J},
	year = {1975},
	pmid = {1200978},
	note = {Place: UNITED STATES
ISBN: 0006-2928},
	keywords = {Anemia, Sickle Cell, Female, Hemoglobin, Sickle, Hemoglobins, Hemoglobins, Abnormal, Humans, Male, Pedigree, Reticulocytes, Sickle Cell Trait, Thalassemia, research support, u.s. gov't, p.h.s.},
	pages = {783--788},
}

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